State
72,820 recalls have nationwide distribution and so reach Oklahoma. 5,785 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,785 recalls naming Oklahoma we have scored against our rubric, 1,031 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,237 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,785 recalls whose distribution notice names Oklahoma specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed across 28 U.S. states and Mexico.
Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.
Spectra Medical Devices is recalling Sodium Chloride Injection ampules because manufacturing issues may have compromised sterility, posing a risk of infection or inflammation to patients.
Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.
Covidien is recalling Dermalon 4-0 sutures because sterile barrier packaging may be perforated or torn, risking biocontamination and infection.
Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.
Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.
Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.
Taylor Farms is recalling specific lots of Subway Shred Lettuce due to potential Cyclospora contamination. The product was distributed to 28 US states and Mexico.
Apollo Care, LLC is recalling specific lots of Semaglutide 20mg vials because they contain nylon and silk-type particulate matter.
529 Commerce, LLC is recalling Aquafaba Powder, Vegan Replacement, because it contains undeclared egg. The product was distributed to 24 states.
Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.
Taylor Farms is recalling specific lots of garden salad mix and lettuce blends due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.
Taylor Farms is recalling specific Marketside iceberg salad products due to potential Cyclospora contamination. Consumers should check lot codes and discard affected items.
FDA is recalling Surgipro II sutures due to potential sterile packaging defects that could cause biocontamination and infection.
FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because bleach concentration may drop below specification, potentially compromising disinfection effectiveness.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Shoolin Pharma Chem LLP is recalling Tadalafil USP 0.500 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Cardinal Health is recalling 616 Presource Kits because they contain sponges with unexpected endotoxin variability.
FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Cardinal Health is recalling specific Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.
Avride Inc. is recalling Automated Driving Systems (ADS) with specific software versions that may cause unsafe lane changes or merging without yielding.